67213-27-8

Basic information

• Product Name: p-methylselenobenzamide
• Synonyms: p-methylselenobenzamide
• CAS NO: 67213-27-8
• Molecular Weight: 198.126
• Mol File: 67213-27-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: p-methylselenobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: p-methylselenobenzamide(67213-27-8)
• EPA Substance Registry System: p-methylselenobenzamide(67213-27-8)

Safety Data

• Hazardous Substances Data: 67213-27-8(Hazardous Substances Data)

Upstream product

• 104-85-8 para-methylbenzonitrile 

Downstream Products

• 69625-86-1 2-(4-Methylphenyl)-4-phenylselenazole 
• 69625-84-9 4-chloromethyl-2-p-tolyl-selenazole 
• 69625-85-0 4-methyl-2-p-tolyl-selenazole 
• 70250-31-6 2,5-di-p-tolyl-[1,3,4]selenadiazole 
• 67213-21-2 5-(p-Tolyl)-3,3-bis(trifluormethyl)-3H-1,2,4-diselenazol 

Relevant articles and documents

Facile synthesis of selenocarboxamides from nitriles using Se/CO/H 2O under atmospheric pressure

Aromatic and aliphatic nitriles can be conveniently converted into the corresponding selenocarboxamides with Se/CO/H2O under atmospheric pressure without use of a base.

A facile preparation of aliphatic and aromatic primary selenoamides using 4-methylselenobenzoate as a new selenating reagent

Aliphatic and aromatic primary selenoamides 2 were isolated by the reaction of the corresponding aliphatic and aromatic nitriles with potassium 4-methylselenobenzoate in the presence of BF3·Et2O in moderate from high yields.

Synthesis of primary selenocarboxamides and conversion of alkyl selenocarboxamides into selenazoles

Nitriles react with sodium hydrogen selenide, pyridine and hydrochloric acid in ethanol to give primary aryl and alkyl selenocarboxamides. The alkyl selenocarboxamides are converted into selenazoles by reaction with phenacyl bromide.